Amlodipine besylate
- Product NDC
- 71335-1032
- 11-digit product format
- 713351032
- Labeler code
- 71335
- Product ID
- 71335-1032_7100f411-9938-43d2-b2c2-f2059e8e35fb
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Amlodipine besylate
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA077955
- Marketing category
- ANDA
- Marketing start
- 2007-11-02
- Marketing end
- 0000-00-00
- Substance
- AMLODIPINE BESYLATE
- Active strength
- 3 mg/1
- Pharmacologic classes
- Calcium Channel Antagonists [MoA], Dihydropyridine Calcium Channel Blocker [EPC], Dihydropyridines [CS]
- NDC exclude flag
- No
- Listing certified through
- 2023-12-31
- Current FDA listing
- Historical FDA.report record
FDA-Initiated Inactive NDC Indexing#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 71335-1032-1 | 71335103201 | 30 TABLET in 1 BOTTLE (71335-1032-1) | 30 tablet | 2021-12-28 | 0000-00-00 | No | No | Current |
| 71335-1032-2 | 71335103202 | 60 TABLET in 1 BOTTLE (71335-1032-2) | 60 tablet | 2021-12-28 | 0000-00-00 | No | No | Current |
| 71335-1032-3 | 71335103203 | 90 TABLET in 1 BOTTLE (71335-1032-3) | 90 tablet | 2019-02-05 | 0000-00-00 | No | No | Current |
| 71335-1032-4 | 71335103204 | 300 TABLET in 1 BOTTLE (71335-1032-4) | 300 tablet | 2021-12-28 | 0000-00-00 | No | No | Current |
| 71335-1032-5 | 71335103205 | 500 TABLET in 1 BOTTLE (71335-1032-5) | 500 tablet | 2021-12-28 | 0000-00-00 | No | No | Current |
| 71335-1032-6 | 71335103206 | 800 TABLET in 1 BOTTLE (71335-1032-6) | 800 tablet | 2021-12-28 | 0000-00-00 | No | No | Current |
| 71335-1032-7 | 71335103207 | 1000 TABLET in 1 BOTTLE (71335-1032-7) | 1000 tablet | 2019-01-07 | 0000-00-00 | No | No | Current |